Resumen
Triple-negative breast cancer (TNBC) tends to occur in younger women, is aggressive and has a poor outcome due to limited therapies. Recent drug trials have shown promise, but only improved TNBC survival by several months. To discover potential new therapeutic targets and pathways, we focused on the known alteration of glycosylation in cancer, and sought to discover TNBC-specific glycogenes and their regulatory pathways. Using an integrative bioinformatics approach, we discovered 34 TNBC-specific candidate glycogenes, and identified the lacto-/neolacto- glycosphingolipid biosynthesis pathway with seven candidate glycogenes as a novel target in TNBC. Furthermore, we identified three transcription factors as potential therapeutic targets: AR, GATA3 and ZNF622. Each TF target three glycogenes in this pathway. Together, this study revealed novel molecular features of TNBC, identifying potential new therapeutic targets.